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首页> 外文期刊>Fish Physiology and Biochemistry >Acute effects of benzo[a]pyrene on liver phase I and II enzymes, and DNA damage on sea bream Sparus aurata
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Acute effects of benzo[a]pyrene on liver phase I and II enzymes, and DNA damage on sea bream Sparus aurata

机译:苯并[a] py对肝脏I和II期酶的急性作用以及DNA对鲷鱼Sparus aurata的破坏

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摘要

In the present study biotransformation and detoxification responses to acute exposure to the polycyclic aromatic hydrocarbons benzo[a]pyrene (B[a]P) were investigated in the liver of Sparus aurata (sea bream). Sexually immature gilthead sea bream were treated by intraperitoneal injection of B[a]P (20 mg kg(-1)) for 6, 12, 24, and 48 h. B[a]P accumulation was quantified in sea bream liver by mean of gas phase chromatography (GPC-MS) after the various exposure periods. The following biological responses were measured: (1) ethoxyresorufin-O-deethylase (EROD) activity, as a phase I biotransformation parameter; (2) liver glutathione S-transferase (GST) activity as a phase II conjugation enzyme. DNA damage was assessed over time using the single-cell gel electrophoresis comet assay. B[a]P bioaccumulation in the liver resulted in a biphasic curve with an increasing uptake up to 5.55 +/- 0.67 microg g(-1) dry weight after only 6 h exposure and 4.67 +/- 0.68 microg g(-1) dry weight after 48 h exposure. EROD activity showed a nonsymmetrical bell-shaped kinetic with a maximum at 24 h and lower but significant activities at 12 and 48 h with respect to control animals. Hepatic GST activities were only significant after 48 h exposure. Comet assay showed an increase in liver cells DNA damage with a maximum after 48 h exposure reaching up to 12.17 % DNA in the tail.
机译:在本研究中,研究了金头鲷(Sparus aurata)(海鲷)肝脏中急性暴露于多环芳烃苯并[a] py(B [a] P)的生物转化和解毒反应。通过腹腔内注射B [a] P(20 mg kg(-1))治疗性不成熟的金头鲷6、12、24和48 h。在不同暴露时间后,通过气相色谱法(GPC-MS)对鲷鱼肝脏中的B [a] P积累进行了定量。测量了以下生物学反应:(1)乙氧基异佛手菌素-O-脱乙基酶(EROD)活性,作为I相生物转化参数; (2)肝谷胱甘肽S-转移酶(GST)活性为II期结合酶。使用单细胞凝胶电泳彗星试验评估DNA损伤随时间的变化。肝脏中B [a] P的生物蓄积导致双相曲线,仅暴露6 h后的干重增加至5.55 +/- 0.67 microg g(-1),而摄取4.67 +/- 0.68 microg g(-1)则增加干重。暴露48小时后的干重。 EROD活性显示出不对称的钟形动力学,相对于对照动物,其在24 h处最大,而在12和48 h处较低但显着。肝GST活性仅在暴露48 h后才有意义。彗星试验显示肝细胞DNA损伤增加,暴露48小时后最大,尾巴中的DNA高达12.17%。

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